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2,2,5-Triphenylfuran-3-one is an organic compound characterized by a furan ring with three phenyl groups attached to the 2, 2, and 5 positions, and a carbonyl group at the 3 position. This molecule is known for its unique structure and potential applications in various chemical and pharmaceutical processes. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. The compound is synthesized through various chemical reactions, often involving the condensation of phenyl groups with furan derivatives. Due to its aromatic nature and the presence of the furan ring, 2,2,5-triphenylfuran-3-one exhibits interesting electronic properties and can be used as a building block in the synthesis of more complex molecules. Its chemical properties and reactivity make it a subject of interest in organic chemistry research, particularly in the development of new materials and pharmaceuticals.

33925-38-1

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33925-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33925-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33925-38:
(7*3)+(6*3)+(5*9)+(4*2)+(3*5)+(2*3)+(1*8)=121
121 % 10 = 1
So 33925-38-1 is a valid CAS Registry Number.

33925-38-1Upstream product

33925-38-1Downstream Products

33925-38-1Relevant academic research and scientific papers

Gold(III)- and platinum(II)-catalyzed domino reaction consisting of heterocyclization and 1,2-migration: Efficient synthesis of highly substituted 3(2H)-furanones

Kirsch, Stefan F.,Binder, Joerg T.,Liebert, Clemence,Menz, Helge

, p. 5878 - 5880 (2006)

(Chemical Equation Presented) PtCl2-catalyzed alkyne activation initiates a domino reaction, in which a heterocyclization is followed by a 1,2-alkyl migration, for the construction of a variety of substituted 3(2H)-furanones. This stereospecifi

Synthesis of heterocyclic systems by transition-metal-catalyzed cyclization-migration reactions - A diversity-oriented strategy for the construction of spirocyclic 3(2H)-furanones and 3-pyrrolones

Binder, Joerg T.,Crone, Benedikt,Kirsch, Stefan F.,Liebert, Clemence,Menz, Helge

, p. 1636 - 1647 (2008/02/06)

Two platinum(II)-catalyzed heterocyclization-migration reactions that provide five-membered heterocycle products are described. With 5 mol-% of PtCl2 as a catalyst, 2-alkynyl-2-hydroxy carbonyl compounds 1 are converted into 3(2H)-furanones 2 a

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